Canonical Allele Identifier: PA2826444635
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 864117
ClinVar RCV Id: RCV001071228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Glu139Val
CA411097519
NM_001257387.2:c.416A>T