Canonical Allele Identifier: PA2825199076
Gene: CRP HGNC NCBI

Linked Data

ClinVar Variation Id: 3061216
ClinVar RCV Id: RCV003982728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000558.2:p.Glu119Asp
CA343454284
NM_000567.3:c.357G>T
CA343454285
NM_000567.3:c.357G>C