Canonical Allele Identifier: PA163958
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140932
ClinVar RCV Id: RCV000129204 RCV000227256 RCV000214585 RCV000765620 RCV001030685 RCV001201286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Ser252Asn
CA163957
NM_007194.4:c.755G>A