Canonical Allele Identifier: PA645427079
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg649Trp
CA6197652
NM_000260.4:c.1945C>T