Canonical Allele Identifier: PA658659723
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1164Val
CA16028993
NM_001127510.3:c.3490A>G