ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA891857274
Gene: COPA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
576697
ClinVar RCV Id:
RCV000699254
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004362.2:p.Glu241Ala
CA343264523
NM_004371.4:c.722A>C