Canonical Allele Identifier: PA916043613
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 651993
ClinVar RCV Id: RCV000807460 RCV003467423 RCV002453813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Thr399Met
CA410914719
NM_001362877.2:c.1196C>T