Canonical Allele Identifier: PA2827988744
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2202Ala
CA045904
NM_001354900.2:c.6604A>G