Allele Registry

Canonical Allele Identifier: PA2830115626

Gene: TNFSF11 HGNC NCBI

ClinVar Variation Id: 312231

HGVS (amino-acid)	Matching Registered Transcripts
NP_143026.1:p.Ser7Leu	CA6967167 NM_033012.4:c.20C>T