Canonical Allele Identifier: PA2827949532
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368407
ClinVar RCV Id: RCV003772579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser290Arg
CA16023216
NM_001354896.2:c.868A>C
CA16023221
NM_001354896.2:c.870T>A
CA16023222
NM_001354896.2:c.870T>G