Canonical Allele Identifier: PA2827474364
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 820670
ClinVar RCV Id: RCV001014356 RCV001047470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Gln69His
CA10168060
NM_001349956.2:c.207G>C
CA411090788
NM_001349956.2:c.207G>T