Canonical Allele Identifier: PA2828028549
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Leu2228Phe
CA013771
NM_001354906.2:c.6682C>T