Canonical Allele Identifier: PA2827968669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu1660Asp
CA16032387
NM_001354898.2:c.4980A>C
CA16032388
NM_001354898.2:c.4980A>T