NM_054027.6(ANKH):c.1141+190TATT[5] AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 8, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001720887.2
Allele description [Variation Report for NM_054027.6(ANKH):c.1141+190TATT[5]]
NM_054027.6(ANKH):c.1141+190TATT[5]
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023