Canonical Allele Identifier: PA1139727841
Gene: RSPH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 475820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333347.1:p.Arg302Gln
CA4075820
NM_001346418.1:c.905G>A