Allele Registry

Canonical Allele Identifier: PA645492519

Gene: TNFRSF11B HGNC NCBI

ClinVar RCV:

RCV000250490

RCV000291754

RCV001651170

ClinVar Variation:

258775

HGVS (amino-acid)	Matching Registered Transcripts
NP_002537.3:p.Asn3Lys	CA4855017 NM_002546.4:c.9C>G CA371921428 NM_002546.4:c.9C>A