Allele Registry

Canonical Allele Identifier: PA645495240

Gene: TNFRSF13B HGNC NCBI

ClinVar RCV:

RCV000312789

RCV000455556

RCV001520146

RCV001540627

ClinVar Variation:

322025

HGVS (amino-acid)	Matching Registered Transcripts
NP_036584.1:p.Pro251Leu	CA8413859 NM_012452.3:c.752C>T