Canonical Allele Identifier: PA2827971745
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2596Cys
CA014123
NM_001354898.2:c.7787C>G