Canonical Allele Identifier: PA2827957610
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 849086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala1117Val
CA16028617
NM_001354897.2:c.3350C>T