Canonical Allele Identifier: PA658818141
Gene: B4GAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 541281
ClinVar RCV Id: RCV001079253 RCV000828148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006867.1:p.Phe382Leu
CA6120440
NM_006876.3:c.1146C>G
CA381416850
NM_006876.3:c.1146C>A
CA381416855
NM_006876.3:c.1144T>C