Canonical Allele Identifier: PA112198
Gene: TNFRSF11A HGNC NCBI

Linked Data

ClinVar Variation Id: 6303
ClinVar RCV Id: RCV000006683 RCV000355051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003830.1:p.Arg129Cys
CA118116
NM_003839.4:c.385C>T