Canonical Allele Identifier: PA1139739596
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 964536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala1718Pro
CA16032478
NM_001354896.2:c.5152G>C