Canonical Allele Identifier: PA2826059404
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315170
ClinVar RCV Id: RCV001773364
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Gln146_Val148del
CA640357305
NM_001169110.1:c.437_445del