Canonical Allele Identifier: PA2827474729
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141340
ClinVar RCV Id: RCV000129825 RCV000204150 RCV001800430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Phe103Leu
CA165150
NM_001349956.2:c.307T>C
CA411090209
NM_001349956.2:c.309T>G
CA411090212
NM_001349956.2:c.309T>A