Canonical Allele Identifier: PA2825115174
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1309833
ClinVar RCV Id: RCV001756901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Phe470Ile
CA381935335
NM_000260.4:c.1408T>A