Canonical Allele Identifier: PA2825637955
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_001120983.2:p.Arg384Pro
CA16023942
NM_001127511.3:c.1151G>C