Canonical Allele Identifier: PA2828023357
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ile1589Val
CA040590
NM_001354903.2:c.4765A>G