Canonical Allele Identifier: PA2825276751
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1035250
ClinVar RCV Id: RCV001338091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Leu96Phe
CA411090338
NM_001005735.2:c.288A>T
CA411090341
NM_001005735.2:c.288A>C