Canonical Allele Identifier: PA2826467781
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 25299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.His212Tyr
CA259545
NM_001258332.2:c.634C>T