Canonical Allele Identifier: PA2828036423
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 970107
ClinVar RCV Id: RCV003652102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp889Gly
CA16027996
NM_001354904.2:c.2666A>G