Canonical Allele Identifier: PA2828001408
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn935Ser
CA16028071
NM_001354902.2:c.2804A>G