Canonical Allele Identifier: PA2826974302
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30201
ClinVar RCV Id: RCV000023121 RCV000377856 RCV002444438 RCV002504820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Lys373del
CA10575547
NM_001317946.2:c.1118_1120del