Canonical Allele Identifier: PA2827996033
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2775152
ClinVar RCV Id: RCV003585136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Glu1640Ala
CA16032472
NM_001354901.2:c.4919A>C