Allele Registry

Canonical Allele Identifier: PA226625

Gene: RS1 HGNC NCBI

ClinVar RCV:

RCV000085250

RCV002477251

ClinVar Variation:

98916

HGVS (amino-acid)	Matching Registered Transcripts
NP_000321.1:p.Glu72Gln	CA226623 NM_000330.3:c.214G>C