Canonical Allele Identifier: PA2827974417
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624846
ClinVar RCV Id: RCV003387067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile610Thr
CA16025499
NM_001354899.2:c.1829T>C