Canonical Allele Identifier: PA645496973
Gene: TNFRSF11A HGNC NCBI

Linked Data

ClinVar Variation Id: 327738
ClinVar RCV Id: RCV000274363 RCV000357332 RCV002278505 RCV002523051
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003830.1:p.Met540Val
CA8984009
NM_003839.4:c.1618A>G