Allele Registry

Canonical Allele Identifier: PA645385535

Gene: RSPH9 HGNC NCBI

ClinVar Variation Id: 357018

HGVS (amino-acid)	Matching Registered Transcripts
NP_689945.2:p.Arg171Gln	CA3828314 NM_152732.5:c.512G>A