Canonical Allele Identifier: PA236058
Gene: SNRNP200 HGNC NCBI

Linked Data

ClinVar Variation Id: 191118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054733.2:p.Gly865Ser
CA236057
NM_014014.5:c.2593G>A