Canonical Allele Identifier: PA2826059395
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3025219
ClinVar RCV Id: RCV003886095
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Ile136Thr
CA412192817
NM_001169110.1:c.407T>C