Canonical Allele Identifier: PA2825199079
Gene: CRP HGNC NCBI

Linked Data

ClinVar Variation Id: 2259287
ClinVar RCV Id: RCV004121295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000558.2:p.Gly166Arg
CA1189166
NM_000567.3:c.496G>A
CA343453911
NM_000567.3:c.496G>C