Allele Registry

Canonical Allele Identifier: PA092609

Gene: RS1 HGNC NCBI

ClinVar RCV:

RCV000010571

RCV001385707

ClinVar Variation:

9893

HGVS (amino-acid)	Matching Registered Transcripts
NP_000321.1:p.Cys223Arg	CA254929 NM_000330.3:c.667T>C