Canonical Allele Identifier: PA2829536385
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_004362.2:p.Leu932Val
CA343274802
NM_004371.4:c.2794C>G