Canonical Allele Identifier: PA2580232217
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1723239
ClinVar RCV Id: RCV002308515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Arg394Thr
CA410914548
NM_001362877.2:c.1181G>C