Canonical Allele Identifier: PA2828028231
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2181Cys
CA16037430
NM_001354906.2:c.6542C>G