Canonical Allele Identifier: PA2499276876
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1047360
ClinVar RCV Id: RCV001352061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036584.1:p.Arg84Thr
CA8414059
NM_012452.3:c.251G>C