Canonical Allele Identifier: PA2827477897
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 126909
ClinVar RCV Id: RCV000114765 RCV000160437 RCV000196666 RCV000515378 RCV000449435 RCV001147096 RCV001356532 RCV001798305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Asn379Asp
CA230682
NM_001349956.2:c.1135A>G