Canonical Allele Identifier: PA2825025118
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 640552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile2666Val
CA16038700
NM_000038.6:c.7996A>G