Canonical Allele Identifier: PA116435
Gene: GALE HGNC NCBI

Linked Data

ClinVar Variation Id: 3682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008217.1:p.Val94Met
CA116434
NM_001008216.2:c.280G>A