Canonical Allele Identifier: PA916041122
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile2242Val
CA012361
NM_001354896.2:c.6724A>G