Allele Registry

Canonical Allele Identifier: PA092711

Gene: RS1 HGNC NCBI

ClinVar RCV:

RCV000085275

ClinVar Variation:

98935

HGVS (amino-acid)	Matching Registered Transcripts
NP_000321.1:p.Gly109Trp	CA226681 NM_000330.3:c.325G>T