Canonical Allele Identifier: PA2826444771
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141136
ClinVar RCV Id: RCV000129508 RCV000206654 RCV000589481 RCV001175352 RCV001357703 RCV003483495 RCV003493452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Ala171Val
CA164560
NM_001257387.2:c.512C>T