Canonical Allele Identifier: PA2826976833
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 2141685
ClinVar RCV Id: RCV003060428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Pro69Ser
CA10270362
NM_001318038.3:c.205C>T