Canonical Allele Identifier: PA2826059354
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1219241
ClinVar RCV Id: RCV001588330 RCV003147639 RCV003235591
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Leu94Pro
CA10321245
NM_001169110.1:c.281T>C