Canonical Allele Identifier: PA891849690
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 572199
ClinVar RCV Id: RCV000693526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Ser40Pro
CA891844565
NM_007194.4:c.118_119delinsCC