Canonical Allele Identifier: PA2828002528
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 665553
ClinVar RCV Id: RCV003653404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile1489Thr
CA16031726
NM_001354902.2:c.4466T>C