Canonical Allele Identifier: PA165092
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141314
ClinVar RCV Id: RCV000129786 RCV000461401 RCV000480654 RCV000780181 RCV003993818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Asp162Gly
CA165091
NM_007194.4:c.485A>G