Canonical Allele Identifier: PA2826059547
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 342128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Leu2Val
CA10651520
NM_001169111.2:c.4C>G