Canonical Allele Identifier: PA2827474061
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2900230
ClinVar RCV Id: RCV003608636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser28Phe
CA411091614
NM_001349956.2:c.83C>T