Canonical Allele Identifier: PA2828027687
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2255Ala
CA046771
NM_001354903.2:c.6763A>G