Canonical Allele Identifier: PA916077053
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 491658
ClinVar RCV Id: RCV000584483 RCV003500578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser31Phe
CA411091561
NM_145862.2:c.92C>T