Canonical Allele Identifier: PA2826973838
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8031
ClinVar RCV Id: RCV000008496 RCV003231093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Glu31Val
CA119236
NM_001317946.2:c.92A>T