Canonical Allele Identifier: PA2827996220
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gln1693Glu
CA16032822
NM_001354901.2:c.5077C>G