Canonical Allele Identifier: PA2826444497
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 491659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Met110Thr
CA411099448
NM_001257387.2:c.329T>C