Canonical Allele Identifier: PA2825025070
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2773680
ClinVar RCV Id: RCV003585653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val2651Ala
CA16038600
NM_000038.6:c.7952T>C