Canonical Allele Identifier: PA2827476561
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479604
ClinVar RCV Id: RCV000562095 RCV001865716 RCV003320192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.His272Arg
CA411097827
NM_001349956.2:c.815A>G