Canonical Allele Identifier: PA2825276717
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 577593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Pro90Ser
CA10168054
NM_001005735.2:c.268C>T