Canonical Allele Identifier: PA2825643898
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2338Ala
CA046771
NM_001127511.3:c.7012A>G