Canonical Allele Identifier: PA2827975986
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 823680
ClinVar Variation Id: 2720472
ClinVar RCV Id: RCV003537888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val1097Leu
CA16028725
NM_001354899.2:c.3289G>C
CA16028726
NM_001354899.2:c.3289G>T