Allele Registry

Canonical Allele Identifier: PA218964

Gene: RS1 HGNC NCBI

ClinVar RCV:

RCV000058877

ClinVar Variation:

68073

HGVS (amino-acid)	Matching Registered Transcripts
NP_000321.1:p.Ile125Arg	CA218962 NM_000330.3:c.374T>G