Canonical Allele Identifier: PA891848924
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 580796
ClinVar RCV Id: RCV000997886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003064.2:p.Thr357Ile
CA410913532
NM_003073.5:c.1070C>T