Canonical Allele Identifier: PA891848896
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 575245
ClinVar RCV Id: RCV000697410 RCV003163216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Cys167Trp
CA410935397
NM_003073.5:c.501C>G