Canonical Allele Identifier: PA645429498
Gene: SNRNP200 HGNC NCBI

Linked Data

ClinVar Variation Id: 337551
ClinVar RCV Id: RCV000284209 RCV001861159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054733.2:p.Ile889Val
CA1778652
NM_014014.5:c.2665A>G