Canonical Allele Identifier: PA2825627475
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ala1717Val
CA6198660
NM_001127180.2:c.5150C>T