Canonical Allele Identifier: PA2828027458
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2217Gly
CA046510
NM_001354903.2:c.6649A>G