Canonical Allele Identifier: PA2828012181
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr2423Ala
CA048361
NM_001354902.2:c.7267A>G