Allele Registry

Canonical Allele Identifier: PA092617

Gene: RS1 HGNC NCBI

ClinVar Allele:

104798

4015741

ClinVar RCV:

RCV000085241

RCV005413252

ClinVar Variation:

98908

3899905

HGVS (amino-acid)	Matching Registered Transcripts
NP_000321.1:p.Cys59Ser	CA226605 NM_000330.3:c.175T>A CA412376053 NM_000330.3:c.176G>C