Canonical Allele Identifier: PA2573243798
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1442338
ClinVar RCV Id: RCV001969837
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Asp219Gly
CA412191590
NM_005138.3:c.656A>G