Canonical Allele Identifier: PA658660464
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly2325Asp
CA16036537
NM_001127510.3:c.6974G>A