Canonical Allele Identifier: PA2826467735
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 3621
ClinVar RCV Id: RCV000003805 RCV000224446 RCV001831510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.Lys176Asn
CA340107
NM_001258332.2:c.528G>T
CA373284303
NM_001258332.2:c.528G>C