Canonical Allele Identifier: PA2825024726
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760236
ClinVar RCV Id: RCV002400612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2569Thr
CA16038070
NM_000038.6:c.7706G>C