Canonical Allele Identifier: PA2826059432
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5680
ClinVar RCV Id: RCV000006034 RCV001851687
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Arg171Trp
CA117676
NM_001169110.1:c.511C>T