Canonical Allele Identifier: PA2826059091
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1511650
ClinVar RCV Id: RCV002020522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162580.1:p.Arg120Pro
CA10321222
NM_001169109.2:c.359G>C