Canonical Allele Identifier: PA916041667
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489502
ClinVar RCV Id: RCV000579772 RCV003537238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2697Ile
CA16038783
NM_001354896.2:c.8090C>T