Canonical Allele Identifier: PA2827950193
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_001341825.1:p.Asn620Thr
CA16025269
NM_001354896.2:c.1859A>C