Canonical Allele Identifier: PA645408042
Gene: B4GAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 235443
ClinVar RCV Id: RCV000224604 RCV001243362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006867.1:p.Leu356Pro
CA10581311
NM_006876.3:c.1067T>C