Canonical Allele Identifier: PA658811122
Gene: TNFSF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 501658
ClinVar RCV Id: RCV000597863 RCV001111745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003692.1:p.Gly28Asp
CA6967115
NM_003701.4:c.83G>A