Canonical Allele Identifier: PA1139741942
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946346
ClinVar RCV Id: RCV003650722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg2688Thr
CA16038730
NM_001354896.2:c.8063G>C