Allele Registry

Canonical Allele Identifier: PA2580448047

Gene: ASB13 HGNC NCBI

ClinVar RCV:

RCV004226444

ClinVar Variation:

2395813

HGVS (amino-acid)	Matching Registered Transcripts
NP_078977.2:p.Arg4Gln	CA202271317 NM_024701.4:c.11G>A