Canonical Allele Identifier: PA299121
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182457
ClinVar RCV Id: RCV000160457 RCV000212444 RCV000230102 RCV000765617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Gly342Ser
CA299120
NM_007194.4:c.1024G>A