Canonical Allele Identifier: PA2826059383
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1311662
ClinVar RCV Id: RCV001752645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Met126Thr
CA10321220
NM_001169110.1:c.377T>C