Canonical Allele Identifier: PA2826973867
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Arg53Leu
CA16616285
NM_001317946.2:c.158G>T