Canonical Allele Identifier: PA2825277205
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 629342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Asn359Lys
CA411099908
NM_001005735.2:c.1077T>G
CA411099910
NM_001005735.2:c.1077T>A