Canonical Allele Identifier: PA913200308
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 627696
ClinVar RCV Id: RCV000771409 RCV003653279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys1762Thr
CA16032881
NM_001127510.3:c.5285A>C