Canonical Allele Identifier: PA2580275546
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1919200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Ser111Cys
CA410933991
NM_003073.5:c.332C>G