Canonical Allele Identifier: PA2827959581
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745303
ClinVar RCV Id: RCV002351472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Glu1709Asp
CA16032475
NM_001354897.2:c.5127G>C
CA16032476
NM_001354897.2:c.5127G>T