Canonical Allele Identifier: PA2828320065
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg658Gln
CA6197663
NM_001369365.1:c.1973G>A