Canonical Allele Identifier: PA2826976878
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 2786201
ClinVar RCV Id: RCV003666327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Arg235Trp
CA10270235
NM_001318038.3:c.703C>T