ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA093255
Gene: SNRNP200
HGNC
NCBI
Linked Data
ClinVar Variation Id:
7928
ClinVar RCV Id:
RCV000008390
RCV000505052
RCV001075824
RCV001091895
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_054733.2:p.Ser1087Leu
CA254265
NM_014014.5:c.3260C>T