Canonical Allele Identifier: PA2828028195
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 658256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2176Cys
CA16037401
NM_001354906.2:c.6527C>G