Canonical Allele Identifier: PA658660518
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482440
ClinVar RCV Id: RCV000568737 RCV003459338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly2383Val
CA047090
NM_001127510.3:c.7148G>T