Canonical Allele Identifier: PA278737
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 178667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Tyr403Cys
CA278736
NM_000260.4:c.1208A>G