Canonical Allele Identifier: PA2825640028
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg1096Leu
CA16028658
NM_001127511.3:c.3287G>T