Canonical Allele Identifier: PA166522
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141818
ClinVar RCV Id: RCV000130486 RCV000206869 RCV000222009 RCV001270242 RCV001175336 RCV001355927 RCV001787089 RCV003448269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Tyr390Ser
CA166521
NM_007194.4:c.1169A>C