Allele Registry

Canonical Allele Identifier: PA218967

Gene: RS1 HGNC NCBI

ClinVar RCV:

RCV000058878

ClinVar Variation:

68074

HGVS (amino-acid)	Matching Registered Transcripts
NP_000321.1:p.Asp126His	CA218965 NM_000330.3:c.376G>C