Allele Registry

Canonical Allele Identifier: PA118570

Gene: TNFRSF11B HGNC NCBI

ClinVar RCV:

RCV000007386

RCV001851721

ClinVar Variation:

6971

HGVS (amino-acid)	Matching Registered Transcripts
NP_002537.3:p.Phe117Leu	CA118569 NM_002546.4:c.349T>C CA371920467 NM_002546.4:c.351C>G CA371920468 NM_002546.4:c.351C>A