Canonical Allele Identifier: PA2826976892
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 2605581
ClinVar RCV Id: RCV004350650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Lys319Asn
CA324732103
NM_001318038.3:c.957G>C
CA411810146
NM_001318038.3:c.957G>T