Canonical Allele Identifier: PA2828001559
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg1023Leu
CA16028658
NM_001354902.2:c.3068G>T