Canonical Allele Identifier: PA2827476321
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 629342
ClinVar RCV Id: RCV000774044 RCV001322772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Asn249Lys
CA411099908
NM_001349956.2:c.747T>G
CA411099910
NM_001349956.2:c.747T>A