Canonical Allele Identifier: PA2499270148
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1056906
ClinVar RCV Id: RCV001365802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Arg95His
CA10321243
NM_005138.3:c.284G>A