Canonical Allele Identifier: PA2580327071
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2012335
ClinVar RCV Id: RCV002843039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Pro138Arg
CA412192802
NM_005138.3:c.413C>G