ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826059099
Gene: SCO2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2630070
ClinVar RCV Id:
RCV003402108
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001162580.1:p.Gly129Ser
CA412192890
NM_001169109.2:c.385G>A