Canonical Allele Identifier: PA2828029259
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2338Cys
CA014123
NM_001354906.2:c.7013C>G