Canonical Allele Identifier: PA2499229092
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 1028105
ClinVar RCV Id: RCV001329065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Phe93Ser
CA373279173
NM_000155.4:c.278T>C