Canonical Allele Identifier: PA645465731
Gene: SCO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 287405
ClinVar RCV Id: RCV000308070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004580.1:p.Arg57Pro
CA8393696
NM_004589.4:c.170G>C