Canonical Allele Identifier: PA2827978143
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1035716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys1742Asn
CA16032941
NM_001354899.2:c.5226G>C
CA16032942
NM_001354899.2:c.5226G>T