Canonical Allele Identifier: PA658675177
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_003064.2:p.Thr372Met
CA322582221
NM_003073.5:c.1115C>T