Canonical Allele Identifier: PA2828319814
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1309833
ClinVar RCV Id: RCV001756901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Phe459Ile
CA381935335
NM_001369365.1:c.1375T>A