Canonical Allele Identifier: PA658807880
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 532968
ClinVar RCV Id: RCV001302083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Arg366His
CA410913862
NM_003073.5:c.1097G>A