Canonical Allele Identifier: PA2573243772
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1384299
ClinVar RCV Id: RCV001895891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Glu154Lys
CA10321200
NM_005138.3:c.460G>A