Canonical Allele Identifier: PA2825637845
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp348Asn
CA026688
NM_001127511.3:c.1042G>A