Canonical Allele Identifier: PA2827941401
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr628Ile
CA029849
NM_001354895.2:c.1883C>T