Canonical Allele Identifier: PA092780
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 9890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Gly74Val
CA226631
NM_000330.3:c.221G>T