Canonical Allele Identifier: PA322191
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 215127
ClinVar RCV Id: RCV000197726 RCV000765657
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Met126Ile
CA322189
NM_005138.3:c.378G>A
CA412192916
NM_005138.3:c.378G>T
CA412192918
NM_005138.3:c.378G>C