Canonical Allele Identifier: PA2827961812
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr2389Pro
CA16036870
NM_001354897.2:c.7165A>C