Canonical Allele Identifier: PA2827980906
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2014516
ClinVar RCV Id: RCV003742946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu2589Asp
CA16038391
NM_001354899.2:c.7767A>C
CA16038392
NM_001354899.2:c.7767A>T