Canonical Allele Identifier: PA2828029313
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2344Phe
CA049365
NM_001354906.2:c.7031C>T