Canonical Allele Identifier: PA299095
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182441
ClinVar RCV Id: RCV000160441 RCV000212471 RCV000476991 RCV001030619 RCV001193688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Ser505Thr
CA299094
NM_007194.4:c.1513T>A