Allele Registry

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Canonical Allele Identifier: PA2826059079

Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1914988

ClinVar RCV Id: RCV002597967

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001162580.1:p.His109Gln	CA10321234 NM_001169109.2:c.327C>G CA412193080 NM_001169109.2:c.327C>A