Allele Registry

Canonical Allele Identifier: PA2828404382

Gene: RGS6 HGNC NCBI

ClinVar RCV:

RCV001665942

ClinVar Variation:

1258962

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357212.1:p.Val478Ile	CA7254309 NM_001370283.1:c.1432G>A