Canonical Allele Identifier: PA2828013096
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2462Thr
CA16038419
NM_001354905.2:c.7384C>A