Canonical Allele Identifier: PA2828003898
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2907983
ClinVar RCV Id: RCV003651671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly2279Asp
CA16036812
NM_001354902.2:c.6836G>A