Canonical Allele Identifier: PA645427777
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 228997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg373Cys
CA10577210
NM_001127180.2:c.1117C>T