Canonical Allele Identifier: PA658819519
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 530218
ClinVar RCV Id: RCV000635959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Val395Ala
CA411096804
NM_007194.4:c.1184T>C