Allele Registry

Canonical Allele Identifier: PA916043604

Gene: SMARCB1 HGNC NCBI

ClinVar RCV:

RCV000194966

RCV000515012

ClinVar Variation:

212263

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