Allele Registry

Canonical Allele Identifier: PA2829403432

Gene: RGS13 HGNC NCBI

ClinVar RCV:

RCV004212746

ClinVar Variation:

2373716

HGVS (amino-acid)	Matching Registered Transcripts
NP_002918.1:p.Pro20Ser	CA1301590 NM_002927.5:c.58C>T