Canonical Allele Identifier: PA351417
Gene: RSPRY1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218886
ClinVar RCV Id: RCV000203224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_588609.1:p.Gly41Cys
CA278754
NM_133368.3:c.121G>T