Canonical Allele Identifier: PA151528
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 128056
ClinVar RCV Id: RCV000115996 RCV000200982 RCV000199565 RCV000587890 RCV000515311 RCV001269492 RCV001356041 RCV001294021 RCV001798350 RCV001147975 RCV004528803 RCV003492502 RCV003483481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Asp438Tyr
CA151527
NM_007194.4:c.1312G>T