Canonical Allele Identifier: PA2826973942
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1443874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Thr109Pro
CA410934083
NM_001317946.2:c.325A>C