Canonical Allele Identifier: PA2828019048
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn925Thr
CA16028070
NM_001354903.2:c.2774A>C