Canonical Allele Identifier: PA645494345
Gene: TNFSF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 312230
ClinVar RCV Id: RCV000335242 RCV003114478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003692.1:p.Val50Met
CA6967139
NM_003701.4:c.148G>A