Canonical Allele Identifier: PA2826059693
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2012335
ClinVar RCV Id: RCV002843039
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Pro138Arg
CA412192802
NM_001169111.2:c.413C>G