Canonical Allele Identifier: PA2827965670
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser762Gly
CA031761
NM_001354898.2:c.2284A>G