Canonical Allele Identifier: PA2828023122
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1391393
ClinVar RCV Id: RCV003772694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly1411Cys
CA16032439
NM_001354906.2:c.4231G>T