Allele Registry

Canonical Allele Identifier: PA915994023

Gene: ARHGEF28 HGNC NCBI

ClinVar RCV:

RCV000243131

RCV001675703

ClinVar Variation:

257376

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171164.1:p.Trp225Arg	CA3304267 NM_001177693.2:c.673T>C CA360110544 NM_001177693.2:c.673T>A