Canonical Allele Identifier: PA2828028778
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_001341835.1:p.Thr2263Ser
CA16037917
NM_001354906.2:c.6787A>T
CA16037919
NM_001354906.2:c.6788C>G