Canonical Allele Identifier: PA2828011998
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 576900
ClinVar RCV Id: RCV003534678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2378Pro
CA16037450
NM_001354902.2:c.7132T>C