Canonical Allele Identifier: PA2825015113
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met466Val
CA027319
NM_000038.6:c.1396A>G