Canonical Allele Identifier: PA2827998086
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gln2263Arg
CA16036522
NM_001354901.2:c.6788A>G