Canonical Allele Identifier: PA2825276671
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 578035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Tyr72Ser
CA10168059
NM_001005735.2:c.215A>C