Canonical Allele Identifier: PA2828012117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2308Pro
CA013665
NM_001354905.2:c.6922T>C