Canonical Allele Identifier: PA645510087
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 438678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Glu450Val
CA381935201
NM_000260.4:c.1349A>T