Canonical Allele Identifier: PA916041262
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile2347Val
CA012738
NM_001354896.2:c.7039A>G