Canonical Allele Identifier: PA645400204
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1690Val
CA040590
NM_001127510.3:c.5068A>G