Canonical Allele Identifier: PA2827992853
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala676Val
CA007259
NM_001354901.2:c.2027C>T