Canonical Allele Identifier: PA2828055335
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn866Ser
CA16028071
NM_001354905.2:c.2597A>G