Allele Registry

Canonical Allele Identifier: PA2829168046

Gene: ARHGEF28 HGNC NCBI

ClinVar RCV:

RCV000243131

RCV001675703

ClinVar Variation:

257376

HGVS (amino-acid)	Matching Registered Transcripts
NP_001375005.1:p.Trp127Arg	CA3304267 NM_001388076.1:c.379T>C CA360110544 NM_001388076.1:c.379T>A