Canonical Allele Identifier: PA2828069472
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Glu31Val
CA119236
NM_001362877.2:c.92A>T