Canonical Allele Identifier: PA2499276877
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1056901
ClinVar RCV Id: RCV001365796 RCV002476669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036584.1:p.Gln95Glu
CA8414053
NM_012452.3:c.283C>G