Allele Registry

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Canonical Allele Identifier: PA2825526401

Gene: COPA HGNC NCBI

Linked Data

ClinVar Variation Id: 933560

ClinVar RCV Id: RCV001201798

ClinVar Variation Id: 1013258

ClinVar RCV Id: RCV001311658

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001091868.1:p.Trp240Arg	CA343264542 NM_001098398.2:c.718T>C CA343264543 NM_001098398.2:c.718T>A