Canonical Allele Identifier: PA2827989552
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758948
ClinVar RCV Id: RCV002385089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val2442Ala
CA16037539
NM_001354900.2:c.7325T>C