Allele Registry

Canonical Allele Identifier: PA2825781284

Gene: PARN HGNC NCBI

ClinVar RCV:

RCV000653142

RCV001756104

RCV004547823

ClinVar Variation:

542670

HGVS (amino-acid)	Matching Registered Transcripts
NP_001127949.1:p.Lys554Glu	CA7911921 NM_001134477.3:c.1660A>G