Canonical Allele Identifier: PA2573198577
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468458
ClinVar RCV Id: RCV001968993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Asn94His
CA410933847
NM_001317946.2:c.280A>C