Canonical Allele Identifier: PA112437
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420003
ClinVar RCV Id: RCV000485499 RCV000569568 RCV000663289 RCV000765618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Thr323Pro
CA16621062
NM_007194.4:c.967A>C