Canonical Allele Identifier: PA117637
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5595
ClinVar RCV Id: RCV000005943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ala17Ser
CA117636
NM_001005735.2:c.49G>T