Canonical Allele Identifier: PA2827945610
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ile1918Val
CA042868
NM_001354895.2:c.5752A>G