Canonical Allele Identifier: PA2827262991
Gene: CRP HGNC NCBI

Linked Data

ClinVar Variation Id: 3077627
ClinVar RCV Id: RCV004369957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001315986.1:p.Leu101Ser
CA1189212
NM_001329057.2:c.302T>C