Canonical Allele Identifier: PA2829536467
Gene: COPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1050931
ClinVar RCV Id: RCV001358903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004362.2:p.Leu1111Met
CA343271148
NM_004371.4:c.3331C>A