Canonical Allele Identifier: PA2827474727
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 481721
ClinVar RCV Id: RCV000562510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Phe103Ile
CA411090230
NM_001349956.2:c.307T>A