Canonical Allele Identifier: PA915980785
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43144

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ala457Val
CA278624
NM_001127180.2:c.1370C>T