Canonical Allele Identifier: PA2828001381
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn926Ser
CA16028012
NM_001354902.2:c.2777A>G