Canonical Allele Identifier: PA645429589
Gene: SNRNP200 HGNC NCBI

Linked Data

ClinVar Variation Id: 337527
ClinVar RCV Id: RCV000263386 RCV003888808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054733.2:p.Arg2009Cys
CA1777843
NM_014014.5:c.6025C>T