Canonical Allele Identifier: PA092429
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 98959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Arg141Cys
CA226728
NM_000330.3:c.421C>T