Canonical Allele Identifier: PA2829411249
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1521059
ClinVar RCV Id: RCV002031074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Asp367His
CA410913874
NM_003073.5:c.1099G>C