Canonical Allele Identifier: PA2825024320
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1345335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Phe2462Ser
CA16037417
NM_000038.6:c.7385T>C