Canonical Allele Identifier: PA2825015243
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490205
ClinVar RCV Id: RCV000582681
ClinVar Variation Id: 1018692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly487Glu
CA16024504
NM_000038.6:c.1460G>A
CA658683406
NM_000038.6:c.1458_1460delinsCGA