Canonical Allele Identifier: PA2826444642
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_001244316.1:p.Asp140Glu
CA411097497
NM_001257387.2:c.420C>G
CA411097500
NM_001257387.2:c.420C>A