Canonical Allele Identifier: PA2828320389
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg922His
CA6197936
NM_001369365.1:c.2765G>A