Canonical Allele Identifier: PA1139739571
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 933607
ClinVar RCV Id: RCV003650655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1706Asn
CA16032401
NM_001354896.2:c.5116G>A