Canonical Allele Identifier: PA2828731021
Gene: RAPGEF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364865.1:p.Tyr522Cys
CA352156
NM_001377936.1:c.1565A>G