Canonical Allele Identifier: PA2827994915
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala1299Val
CA008903
NM_001354901.2:c.3896C>T