Canonical Allele Identifier: PA156826
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp1000Asn
CA008010
NM_001127511.3:c.2998G>A