Canonical Allele Identifier: PA2828029397
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro2521Thr
CA16038419
NM_001354903.2:c.7561C>A