Canonical Allele Identifier: PA2828069568
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 582394
ClinVar RCV Id: RCV001342433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Asp101Gly
CA10145889
NM_001362877.2:c.302A>G