Allele Registry

Canonical Allele Identifier: PA092490

Gene: TNFRSF13B HGNC NCBI

ClinVar RCV:

RCV000005627

RCV000397011

RCV000730698

RCV001532954

ClinVar Variation:

5304

HGVS (amino-acid)	Matching Registered Transcripts
NP_036584.1:p.Arg202His	CA117392 NM_012452.3:c.605G>A