Canonical Allele Identifier: PA2828023319
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_001341835.1:p.Ile1440Val
CA16032626
NM_001354906.2:c.4318A>G