Canonical Allele Identifier: PA2828320959
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43237

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Val1443Ile
CA132320
NM_001369365.1:c.4327G>A