Canonical Allele Identifier: PA2827990148
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1496036
ClinVar RCV Id: RCV003773284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Cys2623Tyr
CA16038688
NM_001354900.2:c.7868G>A