Canonical Allele Identifier: PA2828004788
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513
ClinVar RCV Id: RCV000572880 RCV003537176 RCV004001004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr1000Ala
CA035507
NM_001354905.2:c.2998A>G