Canonical Allele Identifier: PA2580327002
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2062321
ClinVar RCV Id: RCV002953353 RCV003108135
ClinVar Variation Id: 2442147
ClinVar RCV Id: RCV003148476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Gly68Arg
CA325556045
NM_005138.3:c.202G>C
CA412193662
NM_005138.3:c.202G>A