Canonical Allele Identifier: PA916042250
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142278
ClinVar RCV Id: RCV000131302 RCV000167872 RCV000211895 RCV000779725 RCV003534387 RCV003925279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg293Gln
CA015555
NM_001354902.2:c.878G>A