Allele Registry

Canonical Allele Identifier: PA2830300363

Gene: CHEK2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

20637

ClinVar RCV:

RCV000114761

RCV000129670

RCV000233960

RCV000765623

RCV001030688

RCV001149529

RCV001193685

RCV001294022

RCV001357854

RCV001797995

RCV003333687

ClinVar Variation:

5598

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_665861.1:p.Arg181His	CA117641 NM_145862.2:c.542G>A