Canonical Allele Identifier: PA2826059525
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1163688
ClinVar RCV Id: RCV001508948
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Arg255Leu
CA10321112
NM_001169110.1:c.764G>T