Allele Registry

Canonical Allele Identifier: PA092857

Gene: RS1 HGNC NCBI

ClinVar RCV:

RCV000010570

RCV000085290

ClinVar Variation:

9892

HGVS (amino-acid)	Matching Registered Transcripts
NP_000321.1:p.Leu13Pro	CA226709 NM_000330.3:c.38T>C