Canonical Allele Identifier: PA2827998426
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2366Asn
CA16037169
NM_001354901.2:c.7097G>A