Canonical Allele Identifier: PA2825276647
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2753487
ClinVar RCV Id: RCV003500071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Val66Leu
CA411090816
NM_001005735.2:c.196G>T
CA411090818
NM_001005735.2:c.196G>C