Canonical Allele Identifier: PA2827956779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469755
ClinVar RCV Id: RCV001015969 RCV001577894 RCV003767012 RCV003999370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg866Cys
CA032524
NM_001354897.2:c.2596C>T