Canonical Allele Identifier: PA2827952205
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745303
ClinVar RCV Id: RCV002351472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu1717Asp
CA16032475
NM_001354896.2:c.5151G>C
CA16032476
NM_001354896.2:c.5151G>T