Canonical Allele Identifier: PA2826059312
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 618870
ClinVar RCV Id: RCV000757745
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Gly65Ser
CA412193724
NM_001169110.1:c.193G>A