Canonical Allele Identifier: PA916043604
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 212263
ClinVar RCV Id: RCV000194966 RCV000515012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Lys381Glu
CA209485
NM_001362877.2:c.1141A>G