Canonical Allele Identifier: PA2825635376
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761670
ClinVar RCV Id: RCV002419243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg2673Ile
CA16038747
NM_001127510.3:c.8018G>T