Canonical Allele Identifier: PA658660868
Gene: B4GAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 474252
ClinVar RCV Id: RCV000543072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006867.1:p.Pro327Gln
CA381417226
NM_006876.3:c.980C>A