Canonical Allele Identifier: PA916077050
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 822883
ClinVar RCV Id: RCV001018620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Gly30Asp
CA322998843
NM_145862.2:c.89G>A