Canonical Allele Identifier: PA2827474202
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769058
ClinVar RCV Id: RCV002383275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Thr43Ser
CA411091251
NM_001349956.2:c.128C>G
CA411091263
NM_001349956.2:c.127A>T