Canonical Allele Identifier: PA2826059738
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 215128
ClinVar RCV Id: RCV001705133 RCV004020423
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Ala176Val
CA324204
NM_001169111.2:c.527C>T