Canonical Allele Identifier: PA132228
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg623His
CA132227
NM_000260.4:c.1868G>A