Canonical Allele Identifier: PA092450
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 98960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Arg141His
CA226730
NM_000330.3:c.422G>A