Canonical Allele Identifier: PA2827476876
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 240728
ClinVar RCV Id: RCV000227403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Thr300Ser
CA10583902
NM_001349956.2:c.899C>G
CA411097205
NM_001349956.2:c.898A>T