Canonical Allele Identifier: PA2828001350
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp912Asn
CA007992
NM_001354902.2:c.2734G>A