Allele Registry

Canonical Allele Identifier: PA2829473995

Gene: TNFSF13 HGNC NCBI

ClinVar RCV:

RCV001684199

RCV003487676

ClinVar Variation:

1270041

HGVS (amino-acid)	Matching Registered Transcripts
NP_003799.1:p.Asn96Ser	CA8350999 NM_003808.4:c.287A>G