Canonical Allele Identifier: PA2828023269
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2775119
ClinVar RCV Id: RCV003585133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala1578Thr
CA16032343
NM_001354903.2:c.4732G>A