Canonical Allele Identifier: PA2828029120
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2676989
ClinVar RCV Id: RCV003463101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile2312Leu
CA16038237
NM_001354906.2:c.6934A>C