Canonical Allele Identifier: PA916040639
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala1811Gly
CA041747
NM_001354896.2:c.5432C>G