Allele Registry

Canonical Allele Identifier: PA2741940067

Gene: TNFRSF13B HGNC NCBI

ClinVar RCV:

RCV003505504

ClinVar Variation:

2698614

HGVS (amino-acid)	Matching Registered Transcripts
NP_036584.1:p.Ala181Val	CA8413957 NM_012452.3:c.542C>T