Canonical Allele Identifier: PA2826974306
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532968
ClinVar RCV Id: RCV001302083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Arg375His
CA410913862
NM_001317946.2:c.1124G>A