Canonical Allele Identifier: PA645429551
Gene: SNRNP200 HGNC NCBI

Linked Data

ClinVar Variation Id: 337540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054733.2:p.Ile1560Val
CA1778160
NM_014014.5:c.4678A>G