Canonical Allele Identifier: PA2825021346
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745303
ClinVar RCV Id: RCV002351472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu1699Asp
CA16032475
NM_000038.6:c.5097G>C
CA16032476
NM_000038.6:c.5097G>T