Canonical Allele Identifier: PA2826444601
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Asn131Ser
CA10167739
NM_001257387.2:c.392A>G