Canonical Allele Identifier: PA2580466245
Gene: TNFSF11 HGNC NCBI
ClinVar RCV:
RCV002903419
ClinVar Variation:
2044087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_143026.1:p.Ser42Leu
CA249050469
NM_033012.4:c.125C>T