Canonical Allele Identifier: PA2827966140
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Leu897Phe
CA033363
NM_001354898.2:c.2689C>T