Canonical Allele Identifier: PA2825633477
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1474360
ClinVar RCV Id: RCV003773096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1706Leu
CA16032517
NM_001127510.3:c.5117C>T