Canonical Allele Identifier: PA2828321578
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1303075
ClinVar RCV Id: RCV001756574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.His1965Arg
CA381934726
NM_001369365.1:c.5894A>G