Canonical Allele Identifier: PA2827987179
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser1716Tyr
CA16032851
NM_001354900.2:c.5147C>A