Canonical Allele Identifier: PA2825021228
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1671Thr
CA16032296
NM_000038.6:c.5011G>A