Canonical Allele Identifier: PA916043601
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 559897
ClinVar RCV Id: RCV000677690 RCV002422457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Thr375Arg
CA410913531
NM_001362877.2:c.1124C>G