Canonical Allele Identifier: PA915981135
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ser1135Tyr
CA132288
NM_001127180.2:c.3404C>A