Canonical Allele Identifier: PA2830302633
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_665861.1:p.Val434Ala
CA411094501
NM_145862.2:c.1301T>C