Canonical Allele Identifier: PA2827951062
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 849086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala1125Val
CA16028617
NM_001354896.2:c.3374C>T