Canonical Allele Identifier: PA2580375958
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1694830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036584.1:p.Cys89Tyr
CA8414056
NM_012452.3:c.266G>A