Canonical Allele Identifier: PA645399813
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu1322Lys
CA037222
NM_001127510.3:c.3964G>A