Allele Registry

Canonical Allele Identifier: PA151528

Gene: CHEK2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000115996

RCV000199565

RCV000200982

RCV000515311

RCV000587890

RCV001147975

RCV001269492

RCV001294021

RCV001356041

RCV001798350

RCV003483481

RCV003492502

RCV004528803

ClinVar Variation:

128056

Amino-acid Alleles

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