Canonical Allele Identifier: PA2827992869
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala681Thr
CA16026193
NM_001354901.2:c.2041G>A