Canonical Allele Identifier: PA2827990006
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2582Ala
CA16038426
NM_001354900.2:c.7744A>G