Canonical Allele Identifier: PA2828069598
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Leu120Phe
CA10145894
NM_001362877.2:c.358C>T