Canonical Allele Identifier: PA2828023105
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile1407Val
CA040590
NM_001354906.2:c.4219A>G