Canonical Allele Identifier: PA2825021366
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys1704Thr
CA16032502
NM_000038.6:c.5111A>C