Canonical Allele Identifier: PA2828018989
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn743Thr
CA16028070
NM_001354906.2:c.2228A>C