Canonical Allele Identifier: PA2826444598
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142151
ClinVar RCV Id: RCV000131011 RCV000456353 RCV000481469 RCV001292666 RCV001354674 RCV001535600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Glu130Asp
CA167545
NM_001257387.2:c.390G>T
CA411097656
NM_001257387.2:c.390G>C