Canonical Allele Identifier: PA2828000397
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_001341831.1:p.Gly396Glu
CA16024504
NM_001354902.2:c.1187G>A
CA658683406
NM_001354902.2:c.1185_1187delinsCGA