Canonical Allele Identifier: PA2828047756
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758948
ClinVar RCV Id: RCV002385089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Val2357Ala
CA16037539
NM_001354904.2:c.7070T>C