Canonical Allele Identifier: PA2826444456
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231952
ClinVar RCV Id: RCV000215454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Glu100Asp
CA10581059
NM_001257387.2:c.300A>C
CA411099792
NM_001257387.2:c.300A>T