Canonical Allele Identifier: PA2826529247
Gene: TNFRSF11A HGNC NCBI

Linked Data

ClinVar Variation Id: 6302
ClinVar RCV Id: RCV000006682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257880.1:p.Cys175Arg
CA118114
NM_001270951.2:c.523T>C