Canonical Allele Identifier: PA259348
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 38280
ClinVar RCV Id: RCV000022072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Gly83Arg
CA259347
NM_000155.4:c.247G>A
CA373278930
NM_000155.4:c.247G>C