Canonical Allele Identifier: PA2827971102
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2397Ala
CA012961
NM_001354898.2:c.7189A>G