Canonical Allele Identifier: PA2828047652
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2342Pro
CA013665
NM_001354904.2:c.7024T>C