Canonical Allele Identifier: PA1139740683
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 836545
ClinVar RCV Id: RCV002239282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1966Asn
CA16034106
NM_001354896.2:c.5896G>A