Canonical Allele Identifier: PA2826059257
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1473397
ClinVar RCV Id: RCV002005244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Arg6Trp
CA10321318
NM_001169110.1:c.16C>T