Canonical Allele Identifier: PA2827993796
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp959Asn
CA008010
NM_001354901.2:c.2875G>A