Allele Registry

Canonical Allele Identifier: PA2826314096

Gene: PARN HGNC NCBI

ClinVar RCV:

RCV000653142

RCV001756104

RCV004547823

ClinVar Variation:

542670

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229921.1:p.Lys569Glu	CA7911921 NM_001242992.2:c.1705A>G