Canonical Allele Identifier: PA2827999060
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2562Cys
CA014123
NM_001354901.2:c.7685C>G