Canonical Allele Identifier: PA093255
Gene: SNRNP200 HGNC NCBI

Linked Data

ClinVar Variation Id: 7928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054733.2:p.Ser1087Leu
CA254265
NM_014014.5:c.3260C>T