Canonical Allele Identifier: PA2826974310
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1521059
ClinVar RCV Id: RCV002031074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Asp376His
CA410913874
NM_001317946.2:c.1126G>C