Canonical Allele Identifier: PA2825287035
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468458
ClinVar RCV Id: RCV001968993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Asn94His
CA410933847
NM_001007468.3:c.280A>C