Canonical Allele Identifier: PA2828001372
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2135042
ClinVar RCV Id: RCV003745544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His922Pro
CA16027978
NM_001354902.2:c.2765A>C