Canonical Allele Identifier: PA2828012632
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1488918
ClinVar RCV Id: RCV003745503
ClinVar Variation Id: 2773648
ClinVar RCV Id: RCV003584504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr2386Ser
CA16037917
NM_001354905.2:c.7156A>T
CA16037919
NM_001354905.2:c.7157C>G