Canonical Allele Identifier: PA2827474238
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 819021
ClinVar RCV Id: RCV001011203 RCV001038692 RCV001535723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Met46Leu
CA411091161
NM_001349956.2:c.136A>T
CA411091164
NM_001349956.2:c.136A>C