Canonical Allele Identifier: PA645459090
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 265393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Arg366Cys
CA10588715
NM_003073.5:c.1096C>T