Canonical Allele Identifier: PA270109
Gene: SNRNP200 HGNC NCBI

Linked Data

ClinVar Variation Id: 143145
ClinVar RCV Id: RCV000132670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054733.2:p.Val683Leu
CA270108
NM_014014.5:c.2047G>T
CA347679535
NM_014014.5:c.2047G>C