Canonical Allele Identifier: PA2828051914
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr238Ile
CA16023266
NM_001354905.2:c.713C>T