Canonical Allele Identifier: PA118568
Gene: TNFRSF11B HGNC NCBI

Linked Data

ClinVar Variation Id: 6970
ClinVar RCV Id: RCV000007385
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Amino-acid Alleles

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