Canonical Allele Identifier: PA2828069503
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410706
ClinVar RCV Id: RCV000490024 RCV000785603 RCV002402285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Arg53Leu
CA16616285
NM_001362877.2:c.158G>T