Canonical Allele Identifier: PA2828009670
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser1666Tyr
CA16032851
NM_001354902.2:c.4997C>A