Canonical Allele Identifier: PA2827991288
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala160Thr
CA16022765
NM_001354901.2:c.478G>A