Canonical Allele Identifier: PA2825628253
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gly2174Ser
CA132445
NM_001127180.2:c.6520G>A