Canonical Allele Identifier: PA2580217348
Gene: CRP HGNC NCBI

Linked Data

ClinVar Variation Id: 2259287
ClinVar RCV Id: RCV004121295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001315986.1:p.Gly166Arg
CA1189166
NM_001329057.2:c.496G>A
CA343453911
NM_001329057.2:c.496G>C