Canonical Allele Identifier: PA2827622973
Gene: RAPGEF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2615204
ClinVar RCV Id: RCV004354794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338656.1:p.Thr723Ile
CA108901852
NM_001351727.2:c.2168C>T