Canonical Allele Identifier: PA2828012557
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1321396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2373Cys
CA16037837
NM_001354905.2:c.7118C>G