Canonical Allele Identifier: PA2828047620
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2338Cys
CA16037430
NM_001354904.2:c.7013C>G