Canonical Allele Identifier: PA2827996313
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 576430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile1720Val
CA16032994
NM_001354901.2:c.5158A>G