Canonical Allele Identifier: PA2827964540
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381932
ClinVar RCV Id: RCV003745392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg377Pro
CA16023942
NM_001354898.2:c.1130G>C