Canonical Allele Identifier: PA916077012
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 128085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Val25Ala
CA288324
NM_145862.2:c.74T>C