Canonical Allele Identifier: PA2827959818
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp1776Gly
CA16032911
NM_001354897.2:c.5327A>G