Canonical Allele Identifier: PA294226
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141977
ClinVar RCV Id: RCV000130733 RCV000198345 RCV000515236 RCV000589669 RCV000855592 RCV001356295 RCV002225433 RCV004532565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Asn186His
CA294225
NM_007194.4:c.556A>C