Canonical Allele Identifier: PA2827476806
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 822131
ClinVar RCV Id: RCV001017229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Asp294Glu
CA411097497
NM_001349956.2:c.882C>G
CA411097500
NM_001349956.2:c.882C>A