Canonical Allele Identifier: PA2827476472
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 849853
ClinVar RCV Id: RCV001053899
ClinVar Variation Id: 1499768
ClinVar RCV Id: RCV002042417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Met264Ile
CA411099444
NM_001349956.2:c.792G>T
CA411099445
NM_001349956.2:c.792G>C
CA411099446
NM_001349956.2:c.792G>A