Canonical Allele Identifier: PA2828053590
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3222005
ClinVar RCV Id: RCV004513423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn442Thr
CA16025269
NM_001354905.2:c.1325A>C