Canonical Allele Identifier: PA645492531
Gene: TNFRSF11B HGNC NCBI

Linked Data

ClinVar Variation Id: 361691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002537.3:p.Asn233Lys
CA4854849
NM_002546.4:c.699C>A
CA371919369
NM_002546.4:c.699C>G