Canonical Allele Identifier: PA2825633560
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746238
ClinVar RCV Id: RCV002344319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys1744Thr
CA16032764
NM_001127510.3:c.5231A>C