Canonical Allele Identifier: PA916041422
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2482Tyr
CA047889
NM_001354896.2:c.7445C>A