Canonical Allele Identifier: PA645398780
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu241Lys
CA047252
NM_001127510.3:c.721G>A