Canonical Allele Identifier: PA2827989869
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1062362
ClinVar RCV Id: RCV003771188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Glu2538Gly
CA16038130
NM_001354900.2:c.7613A>G