Allele Registry

Canonical Allele Identifier: PA358248

Gene: ARHGEF9 HGNC NCBI

ClinVar Allele:

226995

ClinVar RCV:

RCV000210722

RCV001040965

RCV001786341

ClinVar Variation:

225050

HGVS (amino-acid)	Matching Registered Transcripts
NP_056000.1:p.Arg338Trp	CA358247 NM_015185.3:c.1012C>T