Canonical Allele Identifier: PA2825021364
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1703Arg
CA16032494
NM_000038.6:c.5107G>A
CA16032495
NM_000038.6:c.5107G>C