Allele Registry

Canonical Allele Identifier: PA2826930132

Gene: ARHGAP39 HGNC NCBI

ClinVar Allele:

2220309

ClinVar RCV:

RCV004095732

ClinVar Variation:

2232160

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295136.1:p.Ala891Thr	CA187711113 NM_001308207.1:c.2671G>A