Allele Registry

Canonical Allele Identifier: PA645494348

Gene: TNFSF11 HGNC NCBI

ClinVar Variation Id: 312231

HGVS (amino-acid)	Matching Registered Transcripts
NP_003692.1:p.Ser80Leu	CA6967167 NM_003701.4:c.239C>T