Canonical Allele Identifier: PA1139722040
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 949022
ClinVar RCV Id: RCV001220398 RCV001751422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036584.1:p.Arg14Leu
CA8414158
NM_012452.3:c.41G>T