Canonical Allele Identifier: PA2828002729
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411511
ClinVar RCV Id: RCV000472408 RCV001574379 RCV002339183 RCV004001968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile1599Val
CA040590
NM_001354902.2:c.4795A>G