Canonical Allele Identifier: PA2826059631
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1525924
ClinVar RCV Id: RCV002050475
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Leu78Gln
CA325555955
NM_001169111.2:c.233T>A