Canonical Allele Identifier: PA2828003314
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp1903Val
CA043598
NM_001354902.2:c.5708A>T