Canonical Allele Identifier: PA1139735889
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 849086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala981Val
CA16028617
NM_001354904.2:c.2942C>T