Canonical Allele Identifier: PA2828019099
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727545
ClinVar RCV Id: RCV002325885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp932Glu
CA034409
NM_001354903.2:c.2796T>A
CA16028121
NM_001354903.2:c.2796T>G