Canonical Allele Identifier: PA2826059412
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 706220
ClinVar RCV Id: RCV000876757
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Glu152Asp
CA10321202
NM_001169110.1:c.456A>T
CA412192666
NM_001169110.1:c.456A>C