Canonical Allele Identifier: PA2827954077
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2816057
ClinVar RCV Id: RCV003744141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val2669Asp
CA16038599
NM_001354896.2:c.8006T>A