Canonical Allele Identifier: PA2499270147
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1219241
ClinVar RCV Id: RCV001588330 RCV003147639 RCV003235591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Leu94Pro
CA10321245
NM_005138.3:c.281T>C