Canonical Allele Identifier: PA2828319615
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg291His
CA132454
NM_001369365.1:c.872G>A