Canonical Allele Identifier: PA1139679802
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 958863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Leu618Val
CA381938398
NM_001127180.2:c.1852C>G