Canonical Allele Identifier: PA2827987998
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411501
ClinVar RCV Id: RCV000561606 RCV000590075 RCV000855566 RCV001157264 RCV002526456 RCV003899931 RCV004001965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Tyr1966His
CA043743
NM_001354900.2:c.5896T>C