Canonical Allele Identifier: PA2580327049
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1914988
ClinVar RCV Id: RCV002597967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.His109Gln
CA10321234
NM_005138.3:c.327C>G
CA412193080
NM_005138.3:c.327C>A