Canonical Allele Identifier: PA2828023110
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro1408Leu
CA16032423
NM_001354906.2:c.4223C>T