Canonical Allele Identifier: PA2826974308
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 265393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Arg375Cys
CA10588715
NM_001317946.2:c.1123C>T