Canonical Allele Identifier: PA334835
Gene: COPA HGNC NCBI

Linked Data

ClinVar Variation Id: 199256
ClinVar RCV Id: RCV000180778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091868.1:p.Glu241Lys
CA334834
NM_001098398.2:c.721G>A