Canonical Allele Identifier: PA2828049049
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2914999
ClinVar RCV Id: RCV003652941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg2534Ile
CA049562
NM_001354904.2:c.7601G>T