Canonical Allele Identifier: PA2828019748
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys856Gln
CA008372
NM_001354906.2:c.2566A>C