Canonical Allele Identifier: PA916040261
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala1493Val
CA009538
NM_001354896.2:c.4478C>T