Canonical Allele Identifier: PA2573207888
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1521059
ClinVar RCV Id: RCV002031074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Asp385His
CA410913874
NM_001362877.2:c.1153G>C