Canonical Allele Identifier: PA645494343
Gene: TNFSF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 312229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003692.1:p.Pro36Arg
CA6967125
NM_003701.4:c.107C>G