Canonical Allele Identifier: PA2827947567
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470096
ClinVar RCV Id: RCV003742788

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Leu2511Pro
CA16037704
NM_001354895.2:c.7532T>C