Canonical Allele Identifier: PA2825638896
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1787884
ClinVar RCV Id: RCV002428044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala722Gly
CA16026196
NM_001127511.3:c.2165C>G