Canonical Allele Identifier: PA2825276539
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 629330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ser35Phe
CA411091444
NM_001005735.2:c.104C>T