Allele Registry

Canonical Allele Identifier: PA645480041

Gene: RS1 HGNC NCBI

ClinVar RCV:

RCV000413709

ClinVar Variation:

372497

HGVS (amino-acid)	Matching Registered Transcripts
NP_000321.1:p.Cys223Tyr	CA16043215 NM_000330.3:c.668G>A