Canonical Allele Identifier: PA2829697866
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 970938
ClinVar RCV Id: RCV001246601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Gly37Ser
CA411091426
NM_007194.4:c.109G>A