Canonical Allele Identifier: PA092806
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 98953
ClinVar RCV Id: RCV000085294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Ile136Thr
CA226717
NM_000330.3:c.407T>C