Allele Registry

Canonical Allele Identifier: PA092420

Gene: RS1 HGNC NCBI

ClinVar Allele:

24926

ClinVar RCV:

RCV000010565

RCV000085268

RCV000210291

ClinVar Variation:

9887

HGVS (amino-acid)	Matching Registered Transcripts
NP_000321.1:p.Arg102Trp	CA226667 NM_000330.3:c.304C>T