Canonical Allele Identifier: PA2825287400
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Lys355del
CA10575547
NM_001007468.3:c.1064_1066del