Canonical Allele Identifier: PA1139740889
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 985428
ClinVar RCV Id: RCV001266328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Asp387Val
CA410913974
NM_001362877.2:c.1160A>T