Canonical Allele Identifier: PA2827968909
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140893
ClinVar RCV Id: RCV000129133 RCV002514711 RCV003997484 RCV003650388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala1728Pro
CA009970
NM_001354898.2:c.5182G>C