Canonical Allele Identifier: PA1139683260
Gene: COPA HGNC NCBI

Linked Data

ClinVar Variation Id: 970584
ClinVar RCV Id: RCV001246179 RCV003353264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091868.1:p.Gln1060Glu
CA1197681
NM_001098398.2:c.3178C>G