Allele Registry

Canonical Allele Identifier: PA2828403967

Gene: RGS6 HGNC NCBI

ClinVar RCV:

RCV001665942

ClinVar Variation:

1258962

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357202.1:p.Val515Ile	CA7254309 NM_001370273.1:c.1543G>A