Allele Registry

Canonical Allele Identifier: PA118568

Gene: TNFRSF11B HGNC NCBI

ClinVar Allele:

22009

ClinVar RCV:

RCV000007385

ClinVar Variation:

6970

HGVS (amino-acid)	Matching Registered Transcripts
NP_002537.3:p.Cys87Tyr	CA118567 NM_002546.4:c.260G>A