Canonical Allele Identifier: PA2828029413
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn2523Asp
CA16038432
NM_001354903.2:c.7567A>G