Canonical Allele Identifier: PA658826352
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 557086
ClinVar RCV Id: RCV000673177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.His68Arg
CA373278729
NM_000155.4:c.203A>G