Canonical Allele Identifier: PA916041355
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 583265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2420Lys
CA16037022
NM_001354896.2:c.7260T>A
CA16037023
NM_001354896.2:c.7260T>G