Canonical Allele Identifier: PA2825024941
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2623Ala
CA16038426
NM_000038.6:c.7867A>G