Canonical Allele Identifier: PA2828015955
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile261Thr
CA005403
NM_001354906.2:c.782T>C