Canonical Allele Identifier: PA916041604
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2641Ala
CA16038426
NM_001354896.2:c.7921A>G