Canonical Allele Identifier: PA658660493
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly2362Ala
CA16036765
NM_001127510.3:c.7085G>C