Canonical Allele Identifier: PA2827971300
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1758948
ClinVar RCV Id: RCV002385089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Val2458Ala
CA16037539
NM_001354898.2:c.7373T>C