Canonical Allele Identifier: PA2828027502
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2073Ala
CA046771
NM_001354906.2:c.6217A>G