Canonical Allele Identifier: PA2827991498
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419733

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr222Ala
CA050760
NM_001354901.2:c.664A>G