Canonical Allele Identifier: PA092545
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Arg213Trp
CA226830
NM_000330.3:c.637C>T