Canonical Allele Identifier: PA112431
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 128086
ClinVar RCV Id: RCV000116030 RCV000212436 RCV000206871 RCV000587105 RCV002490783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Ile251Phe
CA288326
NM_007194.4:c.751A>T