Canonical Allele Identifier: PA2825015936
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr628Ile
CA029849
NM_000038.6:c.1883C>T