Canonical Allele Identifier: PA2499234692
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045861
ClinVar RCV Id: RCV001350339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Gln401His
CA411097550
NM_001005735.2:c.1203A>T
CA411097552
NM_001005735.2:c.1203A>C