Canonical Allele Identifier: PA2826059692
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3025219
ClinVar RCV Id: RCV003886095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Ile136Thr
CA412192817
NM_001169111.2:c.407T>C