Allele Registry

Canonical Allele Identifier: PA2826179275

Gene: RSPH9 HGNC NCBI

ClinVar RCV:

RCV000265038

RCV001095134

ClinVar Variation:

357020

HGVS (amino-acid)	Matching Registered Transcripts
NP_001180270.1:p.Leu291Phe	CA3828430 NM_001193341.2:c.871C>T