Canonical Allele Identifier: PA286613
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127298
ClinVar RCV Id: RCV000115096 RCV000758729 RCV003493442 RCV003650371 RCV003997219 RCV002514577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg1589His
CA009743
NM_001127510.3:c.4766G>A