Canonical Allele Identifier: PA2827949540
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1764696
ClinVar RCV Id: RCV002373690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser293Arg
CA16023234
NM_001354896.2:c.877A>C
CA16023240
NM_001354896.2:c.879T>A
CA16023241
NM_001354896.2:c.879T>G