Canonical Allele Identifier: PA2828048274
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2426Cys
CA16037960
NM_001354904.2:c.7276A>T