Canonical Allele Identifier: PA2827476309
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410034
ClinVar RCV Id: RCV000476147 RCV000775770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Val247Leu
CA16616586
NM_001349956.2:c.739G>T
CA411099989
NM_001349956.2:c.739G>C