Canonical Allele Identifier: PA2825628081
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1787830
ClinVar RCV Id: RCV002420102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp739His
CA16026186
NM_001127510.3:c.2215G>C