Canonical Allele Identifier: PA2827941901
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Arg805Gln
CA031897
NM_001354895.2:c.2414G>A