Canonical Allele Identifier: PA2828001389
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp927Asn
CA008010
NM_001354902.2:c.2779G>A