Canonical Allele Identifier: PA092498
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 5302
ClinVar RCV Id: RCV000005623 RCV000005624 RCV000302082 RCV000403933 RCV000507544 RCV000735370 RCV001374734 RCV001535526 RCV001526850 RCV002054418 RCV002283439 RCV003398448 RCV003448244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036584.1:p.Cys104Arg
CA117387
NM_012452.3:c.310T>C