Canonical Allele Identifier: PA2828022921
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1988396
ClinVar RCV Id: RCV003776978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr1372Pro
CA16032197
NM_001354906.2:c.4114A>C