Canonical Allele Identifier: PA916077068
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 530035
ClinVar RCV Id: RCV000635617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Gly37Val
CA322998834
NM_145862.2:c.110G>T