Canonical Allele Identifier: PA916006063
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 641589
ClinVar RCV Id: RCV000794862 RCV002536987
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036584.1:p.Gly76Asp
CA8414063
NM_012452.3:c.227G>A