Canonical Allele Identifier: PA093176
Gene: SNRNP200 HGNC NCBI

Linked Data

ClinVar Variation Id: 39746
ClinVar RCV Id: RCV000032962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054733.2:p.Arg1090Leu
CA261210
NM_014014.5:c.3269G>T