Canonical Allele Identifier: PA2828028481
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2214Leu
CA013717
NM_001354906.2:c.6641C>T