Canonical Allele Identifier: PA916006071
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 808238
ClinVar RCV Id: RCV000996501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036584.1:p.Cys86Ser
CA398520134
NM_012452.3:c.257G>C
CA398520139
NM_012452.3:c.256T>A