Canonical Allele Identifier: PA2827947812
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2676783
ClinVar RCV Id: RCV003470242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Lys2585Glu
CA16038170
NM_001354895.2:c.7753A>G