Canonical Allele Identifier: PA2573224606
Gene: TNFRSF11B HGNC NCBI

Linked Data

ClinVar Variation Id: 1511978
ClinVar RCV Id: RCV002016965 RCV003289388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002537.3:p.Val61Met
CA4854973
NM_002546.4:c.181G>A