Canonical Allele Identifier: PA2827982941
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1494734
ClinVar RCV Id: RCV003773269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile387Thr
CA16024233
NM_001354900.2:c.1160T>C