Canonical Allele Identifier: PA2827996357
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala1734Gly
CA041747
NM_001354901.2:c.5201C>G