Canonical Allele Identifier: PA322190
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 215127
ClinVar RCV Id: RCV000197726 RCV000765657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162580.1:p.Met126Ile
CA322189
NM_001169109.2:c.378G>A
CA412192916
NM_001169109.2:c.378G>T
CA412192918
NM_001169109.2:c.378G>C