Canonical Allele Identifier: PA117638
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5595
ClinVar RCV Id: RCV000005943
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Ala17Ser
CA117636
NM_007194.4:c.49G>T