Canonical Allele Identifier: PA2826976836
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 2292353
ClinVar RCV Id: RCV004142384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Glu83Gln
CA10270355
NM_001318038.3:c.247G>C