Canonical Allele Identifier: PA2825638606
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr610Ile
CA029849
NM_001127511.3:c.1829C>T