Canonical Allele Identifier: PA916043606
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532968
ClinVar RCV Id: RCV001302083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Arg384His
CA410913862
NM_001362877.2:c.1151G>A