Allele Registry

Canonical Allele Identifier: PA2826226279

Gene: TNFSF13 HGNC NCBI

ClinVar RCV:

RCV001539204

RCV003487442

ClinVar Variation:

1181749

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185553.1:p.Gly50Arg	CA8350964 NM_001198624.2:c.148G>A CA397868518 NM_001198624.2:c.148G>C