Canonical Allele Identifier: PA916043605
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 265393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Arg384Cys
CA10588715
NM_001362877.2:c.1150C>T