Canonical Allele Identifier: PA645401393
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile2135Val
CA044550
NM_001127510.3:c.6403A>G