Canonical Allele Identifier: PA2828047851
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2371Leu
CA013717
NM_001354904.2:c.7112C>T