Canonical Allele Identifier: PA2827981081
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761533
ClinVar RCV Id: RCV002419106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2639Tyr
CA16038708
NM_001354899.2:c.7915A>T