Canonical Allele Identifier: PA891849696
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 572799
ClinVar RCV Id: RCV000694276 RCV001011845 RCV003320478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Ser50Arg
CA411091013
NM_007194.4:c.150C>G
CA411091016
NM_007194.4:c.150C>A
CA411091034
NM_007194.4:c.148A>C