Canonical Allele Identifier: PA2827959667
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 661458
ClinVar RCV Id: RCV003537282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile1733Val
CA16032626
NM_001354897.2:c.5197A>G