Canonical Allele Identifier: PA2827476141
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 128087
ClinVar RCV Id: RCV000116031 RCV000212438 RCV000464095 RCV000780183 RCV001357959 RCV002477286 RCV004529944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Glu235Asp
CA288327
NM_001349956.2:c.705A>C
CA411100896
NM_001349956.2:c.705A>T