Canonical Allele Identifier: PA2828001401
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2562359
ClinVar RCV Id: RCV003310419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu930Ile
CA16028037
NM_001354902.2:c.2788C>A