Canonical Allele Identifier: PA2826059696
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2095570
ClinVar RCV Id: RCV003012395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Asp139Glu
CA10321211
NM_001169111.2:c.417C>G
CA412192794
NM_001169111.2:c.417C>A