Canonical Allele Identifier: PA2828001760
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gln1102Arg
CA16029193
NM_001354902.2:c.3305A>G