Canonical Allele Identifier: PA104617
Gene: GALE HGNC NCBI

Linked Data

ClinVar Variation Id: 21171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000394.2:p.Arg169Trp
CA341697
NM_000403.4:c.505C>T