Canonical Allele Identifier: PA2829411261
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 638627
ClinVar RCV Id: RCV000791312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Arg377Gly
CA410914598
NM_003073.5:c.1129C>G