Canonical Allele Identifier: PA2825287410
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1521059
ClinVar RCV Id: RCV002031074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007469.1:p.Asp358His
CA410913874
NM_001007468.3:c.1072G>C