Canonical Allele Identifier: PA132256
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg853His
CA132255
NM_000260.4:c.2558G>A