Canonical Allele Identifier: PA2826059385
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444972
ClinVar RCV Id: RCV001958161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162581.1:p.Gly129Ala
CA412192883
NM_001169110.1:c.386G>C