Canonical Allele Identifier: PA2499252868
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000534
ClinVar RCV Id: RCV001296679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Leu396Phe
CA410914622
NM_001362877.2:c.1186C>T