Canonical Allele Identifier: PA2826059268
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1900684
ClinVar RCV Id: RCV002585822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Arg20Leu
CA10321306
NM_001169110.1:c.59G>T