Canonical Allele Identifier: PA148616
Gene: SNRNP200 HGNC NCBI

Linked Data

ClinVar Variation Id: 95552
ClinVar RCV Id: RCV000081583 RCV000953243 RCV000986789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054733.2:p.Val1389Ile
CA148615
NM_014014.5:c.4165G>A