Canonical Allele Identifier: PA645429434
Gene: SNRNP200 HGNC NCBI

Linked Data

ClinVar Variation Id: 337558
ClinVar RCV Id: RCV000404781 RCV001321090 RCV002519995 RCV003888812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054733.2:p.Arg383His
CA1778990
NM_014014.5:c.1148G>A