Canonical Allele Identifier: PA2825024841
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2733518
ClinVar RCV Id: RCV003535123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly2597Leu
CA2697546408
NM_000038.6:c.7789_7790delinsTT