Canonical Allele Identifier: PA2825067978
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 1502471
ClinVar RCV Id: RCV002022361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Ser135Ala
CA373280650
NM_000155.4:c.403T>G