Canonical Allele Identifier: PA2827966747
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 849086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala1082Val
CA16028617
NM_001354898.2:c.3245C>T