Canonical Allele Identifier: PA2580232214
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780323
ClinVar RCV Id: RCV002407840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Glu372Gly
CA410913469
NM_001362877.2:c.1115A>G