Canonical Allele Identifier: PA156827
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1018Asn
CA008010
NM_000038.6:c.3052G>A