Canonical Allele Identifier: PA2827942616
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1018Asn
CA008010
NM_001354895.2:c.3052G>A