Canonical Allele Identifier: PA915984645
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 92520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.Trp81Arg
CA266761
NM_001258332.2:c.241T>C
CA373281798
NM_001258332.2:c.241T>A