ClinGen Allele Registry
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Canonical Allele Identifier:
PA117678
Gene: SCO2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
20720
ClinVar RCV:
RCV000006035
RCV000043619
RCV000198477
RCV000626777
RCV001610286
ClinVar Variation:
5681
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005129.2:p.Glu140Lys
CA117677
NM_005138.3:c.418G>A