Canonical Allele Identifier: PA1139740894
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 916053
ClinVar RCV Id: RCV001171554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Leu396Pro
CA410914631
NM_001362877.2:c.1187T>C