Canonical Allele Identifier: PA2827994089
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg1055Leu
CA16028658
NM_001354901.2:c.3164G>T