Canonical Allele Identifier: PA2825016703
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser787Gly
CA031761
NM_000038.6:c.2359A>G