Canonical Allele Identifier: PA093225
Gene: SNRNP200 HGNC NCBI

Linked Data

ClinVar Variation Id: 39747
ClinVar RCV Id: RCV000032963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054733.2:p.Gln885Glu
CA261211
NM_014014.5:c.2653C>G