Canonical Allele Identifier: PA286587
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1312Ala
CA008783
NM_000038.6:c.3935G>C