Canonical Allele Identifier: PA341698
Gene: GALE HGNC NCBI

Linked Data

ClinVar Variation Id: 21171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008217.1:p.Arg169Trp
CA341697
NM_001008216.2:c.505C>T