Canonical Allele Identifier: PA2828012063
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1345335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Phe2302Ser
CA16037417
NM_001354905.2:c.6905T>C