Canonical Allele Identifier: PA2829466905
Gene: TNFSF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2044087
ClinVar RCV Id: RCV002903419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003692.1:p.Ser115Leu
CA249050469
NM_003701.4:c.344C>T