Canonical Allele Identifier: PA1139737975
Gene: GAL HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057057.2:p.Ala6Thr
CA6151398
NM_015973.5:c.16G>A