Allele Registry

Canonical Allele Identifier: PA2825781162

Gene: PARN HGNC NCBI

ClinVar RCV:

RCV000484657

RCV001308486

RCV002509408

ClinVar Variation:

423824

HGVS (amino-acid)	Matching Registered Transcripts
NP_001127949.1:p.Arg383Cys	CA7912056 NM_001134477.3:c.1147C>T