Canonical Allele Identifier: PA2828032394
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro315Thr
CA16024197
NM_001354904.2:c.943C>A