Canonical Allele Identifier: PA2828319858
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gly508Asp
CA278629
NM_001369365.1:c.1523G>A