Canonical Allele Identifier: PA2741914416
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_005129.2:p.Ile136Thr
CA412192817
NM_005138.3:c.407T>C