Canonical Allele Identifier: PA2826059817
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374485
ClinVar RCV Id: RCV001883113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Asp252Glu
CA10321116
NM_001169111.2:c.756C>G
CA412190367
NM_001169111.2:c.756C>A