Allele Registry

Canonical Allele Identifier: PA117391

Gene: TNFRSF13B HGNC NCBI

ClinVar RCV:

RCV000005625

RCV000005626

RCV000255118

RCV000999848

RCV001199863

RCV002054419

RCV002251881

ClinVar Variation:

5303

HGVS (amino-acid)	Matching Registered Transcripts
NP_036584.1:p.Ala181Glu	CA117389 NM_012452.3:c.542C>A