Canonical Allele Identifier: PA915984709
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 650599
ClinVar RCV Id: RCV000805776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.Gln97Arg
CA373282050
NM_001258332.2:c.290A>G