Canonical Allele Identifier: PA2825276732
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182447
ClinVar RCV Id: RCV000160447 RCV000205700 RCV001354516 RCV000212409
ClinVar Variation Id: 460821
ClinVar RCV Id: RCV000538696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Trp93Arg
CA299105
NM_001005735.2:c.277T>C
CA411090411
NM_001005735.2:c.277T>A