Canonical Allele Identifier: PA645510009
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 439749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.His77Asn
CA373281673
NM_001258332.2:c.229C>A