Canonical Allele Identifier: PA2829411247
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1343154
ClinVar RCV Id: RCV001843755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Arg366Gly
CA410913856
NM_003073.5:c.1096C>G