Canonical Allele Identifier: PA2825025177
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2679Ile
CA16038783
NM_000038.6:c.8036C>T