Canonical Allele Identifier: PA2741826914
Gene: COPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2964744
ClinVar RCV Id: RCV003828366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091868.1:p.Leu941Val
CA343274802
NM_001098398.2:c.2821C>G