Canonical Allele Identifier: PA916040607
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469997
ClinVar RCV Id: RCV003742731 RCV002350316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr1791Ile
CA16032962
NM_001354896.2:c.5372C>T