Canonical Allele Identifier: PA2828017066
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624857
ClinVar RCV Id: RCV003387078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys455Gln
CA16026177
NM_001354906.2:c.1363A>C