Canonical Allele Identifier: PA2827959787
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser1767Tyr
CA16032851
NM_001354897.2:c.5300C>A