Canonical Allele Identifier: PA166822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141931
ClinVar RCV Id: RCV000130647 RCV000198116 RCV000586043 RCV002243795 RCV003905232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His1897Pro
CA010592
NM_000038.6:c.5690A>C