Canonical Allele Identifier: PA164327
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu2589Gly
CA014023
NM_000038.6:c.7766A>G