Canonical Allele Identifier: PA2827474047
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 949613
ClinVar RCV Id: RCV001221109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Gln27His
CA411091632
NM_001349956.2:c.81G>T
CA411091634
NM_001349956.2:c.81G>C