Canonical Allele Identifier: PA2825287058
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1443874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Thr109Pro
CA410934083
NM_001007468.3:c.325A>C