Canonical Allele Identifier: PA891857270
Gene: COPA HGNC NCBI

Linked Data

ClinVar Variation Id: 577775
ClinVar RCV Id: RCV000700608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004362.2:p.Ala239Pro
CA343264564
NM_004371.4:c.715G>C