Canonical Allele Identifier: PA2826903374
Gene: RSPRY1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218886
ClinVar RCV Id: RCV000203224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001292111.1:p.Gly41Cys
CA278754
NM_001305182.2:c.121G>T