Canonical Allele Identifier: PA2828019050
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn925Ser
CA16028071
NM_001354903.2:c.2774A>G