Canonical Allele Identifier: PA2825016787
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg805Gln
CA031897
NM_000038.6:c.2414G>A