Canonical Allele Identifier: PA2580307442
Gene: COPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1928121
ClinVar RCV Id: RCV002614371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004362.2:p.Arg281Trp
CA343263405
NM_004371.4:c.841C>T