Canonical Allele Identifier: PA2827478077
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2064674
ClinVar RCV Id: RCV002953602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Val396Ala
CA411094501
NM_001349956.2:c.1187T>C