Canonical Allele Identifier: PA916077129
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 659407
ClinVar RCV Id: RCV000816408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Glu64Gly
CA411090833
NM_145862.2:c.191A>G