Canonical Allele Identifier: PA645496788
Gene: TNFRSF11A HGNC NCBI

Linked Data

ClinVar Variation Id: 327725
ClinVar RCV Id: RCV000283697 RCV000341445 RCV003765898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003830.1:p.Arg23Gln
CA10648056
NM_003839.4:c.68G>A