Canonical Allele Identifier: PA916043607
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 464321
ClinVar RCV Id: RCV000539836 RCV000561787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349806.1:p.Thr390Met
CA322582221
NM_001362877.2:c.1169C>T