Canonical Allele Identifier: PA2828003259
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350416
ClinVar RCV Id: RCV000332846 RCV000567246 RCV003320183 RCV003535690 RCV003995884 RCV002480220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His1874Pro
CA043314
NM_001354902.2:c.5621A>C