Canonical Allele Identifier: PA2828022803
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 183069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp1353Tyr
CA009798
NM_001354906.2:c.4057G>T