Canonical Allele Identifier: PA645459074
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410706
ClinVar RCV Id: RCV000490024 RCV000785603 RCV002402285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Arg53Leu
CA16616285
NM_003073.5:c.158G>T