Canonical Allele Identifier: PA182409
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 178478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ile376Val
CA182408
NM_000260.4:c.1126A>G