Canonical Allele Identifier: PA2826059555
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2487548
ClinVar RCV Id: RCV003195452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Ser7Arg
CA10321317
NM_001169111.2:c.21C>A
CA412194683
NM_001169111.2:c.21C>G
CA412194694
NM_001169111.2:c.19A>C