Canonical Allele Identifier: PA2827952274
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser1775Tyr
CA16032851
NM_001354896.2:c.5324C>A