Canonical Allele Identifier: PA2826976887
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 1049089
ClinVar RCV Id: RCV001354732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Asp298Tyr
CA10270192
NM_001318038.3:c.892G>T