Canonical Allele Identifier: PA2828048783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro2496Thr
CA16038419
NM_001354904.2:c.7486C>A