Allele Registry

Canonical Allele Identifier: PA264806

Gene: RSPH9 HGNC NCBI

ClinVar RCV:

RCV000057516

RCV000234192

RCV000487186

ClinVar Variation:

66994

HGVS (amino-acid)	Matching Registered Transcripts
NP_689945.2:p.Lys268del	CA264805 NM_152732.5:c.804_806del