Canonical Allele Identifier: PA2826059036
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516382
ClinVar RCV Id: RCV002040833 RCV004046860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162580.1:p.Gly70Ala
CA412193628
NM_001169109.2:c.209G>C