Canonical Allele Identifier: PA916040398
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411531
ClinVar RCV Id: RCV000775710 RCV002230597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala1613Ser
CA16031815
NM_001354896.2:c.4837G>T