Allele Registry

Canonical Allele Identifier: PA2826179271

Gene: RSPH9 HGNC NCBI

ClinVar RCV:

RCV000057516

RCV000234192

RCV000487186

ClinVar Variation:

66994

HGVS (amino-acid)	Matching Registered Transcripts
NP_001180270.1:p.Glu286del	CA264805 NM_001193341.2:c.856_858del