Canonical Allele Identifier: PA2826059615
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2062321
ClinVar RCV Id: RCV002953353 RCV003108135
ClinVar Variation Id: 2442147
ClinVar RCV Id: RCV003148476
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Gly68Arg
CA325556045
NM_001169111.2:c.202G>C
CA412193662
NM_001169111.2:c.202G>A