Canonical Allele Identifier: PA2828024047
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser1559Thr
CA042221
NM_001354906.2:c.4675T>A