Canonical Allele Identifier: PA2827953337
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2676783
ClinVar RCV Id: RCV003470242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys2603Glu
CA16038170
NM_001354896.2:c.7807A>G