Canonical Allele Identifier: PA2828319785
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 438678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Glu439Val
CA381935201
NM_001369365.1:c.1316A>T