Canonical Allele Identifier: PA2825021133
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717783
ClinVar RCV Id: RCV003743871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1646Arg
CA16032141
NM_000038.6:c.4936G>A
CA16032142
NM_000038.6:c.4936G>C