Canonical Allele Identifier: PA2825636401
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2707798
ClinVar RCV Id: RCV003536455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1697Ile
CA16032461
NM_001127510.3:c.5090C>T