Canonical Allele Identifier: PA2826467772
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 3613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.Asn205Asp
CA116380
NM_001258332.2:c.613A>G