Canonical Allele Identifier: PA195739
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Ser35Cys
CA195738
NM_007194.4:c.104C>G