Canonical Allele Identifier: PA2828004308
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2533Asp
CA16038432
NM_001354902.2:c.7597A>G