Canonical Allele Identifier: PA2827977836
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1479573
ClinVar RCV Id: RCV003773137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu1655Gly
CA16032370
NM_001354899.2:c.4964A>G