Allele Registry

Canonical Allele Identifier: PA165092

Gene: CHEK2 HGNC NCBI

ClinVar Allele:

151028

ClinVar RCV:

RCV000129786

RCV000461401

RCV000480654

RCV000780181

RCV003993818

ClinVar Variation:

141314

HGVS (amino-acid)	Matching Registered Transcripts
NP_009125.1:p.Asp162Gly	CA165091 NM_007194.4:c.485A>G