ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825526400
Gene: COPA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
577775
ClinVar RCV Id:
RCV000700608
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001091868.1:p.Ala239Pro
CA343264564
NM_001098398.2:c.715G>C