Canonical Allele Identifier: PA2829697885
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769058
ClinVar RCV Id: RCV002383275

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Thr43Ser
CA411091251
NM_007194.4:c.128C>G
CA411091263
NM_007194.4:c.127A>T