Canonical Allele Identifier: PA2829700047
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_009125.1:p.Gln358His
CA411097550
NM_007194.4:c.1074A>T
CA411097552
NM_007194.4:c.1074A>C