Canonical Allele Identifier: PA2828001128
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly786Ala
CA032861
NM_001354902.2:c.2357G>C