Allele Registry

Canonical Allele Identifier: PA092688

Gene: RS1 HGNC NCBI

ClinVar RCV:

RCV000010569

RCV000085274

RCV001209952

ClinVar Variation:

9891

940378

HGVS (amino-acid)	Matching Registered Transcripts
NP_000321.1:p.Gly109Arg	CA226679 NM_000330.3:c.325G>C CA412372642 NM_000330.3:c.325G>A