ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826059260
Gene: SCO2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
3158630
ClinVar RCV Id:
RCV004455004
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001162581.1:p.Thr9Arg
CA10321315
NM_001169110.1:c.26C>G