Canonical Allele Identifier: PA2825635339
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3071949
ClinVar RCV Id: RCV004011979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile2661Thr
CA16038666
NM_001127510.3:c.7982T>C