Canonical Allele Identifier: PA2827965537
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala715Thr
CA16026193
NM_001354898.2:c.2143G>A