Canonical Allele Identifier: PA2828029749
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761661
ClinVar RCV Id: RCV002419234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly2571Ala
CA16038742
NM_001354903.2:c.7712G>C