Canonical Allele Identifier: PA2825638222
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp473Asn
CA16024524
NM_001127511.3:c.1417G>A