Canonical Allele Identifier: PA2827622910
Gene: RAPGEF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2615204
ClinVar RCV Id: RCV004354794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338655.1:p.Thr768Ile
CA108901852
NM_001351726.3:c.2303C>T