Canonical Allele Identifier: PA2826973848
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 88893
ClinVar RCV Id: RCV000074462 RCV000262341 RCV001533133 RCV004556052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Arg37His
CA145398
NM_001317946.2:c.110G>A