Canonical Allele Identifier: PA2828069597
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1443874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Thr118Pro
CA410934083
NM_001362877.2:c.352A>C