Canonical Allele Identifier: PA916039724
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala715Val
CA030702
NM_001354896.2:c.2144C>T