Canonical Allele Identifier: PA916077057
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 629330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser35Phe
CA411091444
NM_145862.2:c.104C>T