Canonical Allele Identifier: PA2827973987
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp463Glu
CA16024530
NM_001354899.2:c.1389C>A
CA16024531
NM_001354899.2:c.1389C>G