Canonical Allele Identifier: PA658660870
Gene: B4GAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 474247
ClinVar RCV Id: RCV000548189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006867.1:p.Thr337Ser
CA381417164
NM_006876.3:c.1010C>G
CA381417167
NM_006876.3:c.1009A>T