Canonical Allele Identifier: PA2826974319
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1723239
ClinVar RCV Id: RCV002308515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Arg385Thr
CA410914548
NM_001317946.2:c.1154G>C