Canonical Allele Identifier: PA915981410
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43237

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Val1454Ile
CA132320
NM_001127180.2:c.4360G>A