Canonical Allele Identifier: PA2827979667
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2215Ala
CA045904
NM_001354899.2:c.6643A>G