Canonical Allele Identifier: PA2827976017
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2852532
ClinVar RCV Id: RCV003743093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp1105Gly
CA16028780
NM_001354899.2:c.3314A>G