Canonical Allele Identifier: PA2827988809
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro2220Leu
CA012518
NM_001354900.2:c.6659C>T