Allele Registry

Canonical Allele Identifier: PA2830343201

Gene: TNFSF12-TNFSF13 HGNC NCBI

ClinVar RCV:

RCV001684199

RCV003487676

ClinVar Variation:

1270041

HGVS (amino-acid)	Matching Registered Transcripts
NP_742086.1:p.Asn176Ser	CA8350999 NM_172089.4:c.527A>G