Canonical Allele Identifier: PA2827998548
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2405Tyr
CA047889
NM_001354901.2:c.7214C>A