Canonical Allele Identifier: PA658826356
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 550862
ClinVar RCV Id: RCV000665734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Ala191Asp
CA373281836
NM_000155.4:c.572C>A