Canonical Allele Identifier: PA2828025296
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp1753Asn
CA16034696
NM_001354906.2:c.5257G>A