Canonical Allele Identifier: PA128773
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 29926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg395His
CA128772
NM_000260.4:c.1184G>A