Canonical Allele Identifier: PA2825024408
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758948
ClinVar RCV Id: RCV002385089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val2483Ala
CA16037539
NM_000038.6:c.7448T>C