Canonical Allele Identifier: PA2573243770
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1520040
ClinVar RCV Id: RCV002038496
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Arg149Gln
CA10321204
NM_005138.3:c.446G>A