Allele Registry

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Canonical Allele Identifier: PA2826059318

Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2062321

ClinVar RCV Id: RCV002953353 RCV003108135

ClinVar Variation Id: 2442147

ClinVar RCV Id: RCV003148476

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001162581.1:p.Gly68Arg	CA325556045 NM_001169110.1:c.202G>C CA412193662 NM_001169110.1:c.202G>A