Canonical Allele Identifier: PA2828003078
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp1780Tyr
CA042401
NM_001354902.2:c.5338G>T