Canonical Allele Identifier: PA2828042938
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1332383
ClinVar RCV Id: RCV001805429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr1647Pro
CA16032957
NM_001354904.2:c.4939A>C