Canonical Allele Identifier: PA099372
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg212His
CA277961
NM_000260.4:c.635G>A