Canonical Allele Identifier: PA16040023
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1793Gly
CA041747
NM_000038.6:c.5378C>G