Canonical Allele Identifier: PA2580198665
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714604
ClinVar RCV Id: RCV002295696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Lys99Arg
CA410933942
NM_001317946.2:c.296A>G