Canonical Allele Identifier: PA2828019772
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn859Thr
CA035313
NM_001354906.2:c.2576A>C