Canonical Allele Identifier: PA2827951341
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gln1211Arg
CA16029193
NM_001354896.2:c.3632A>G