Allele Registry

Canonical Allele Identifier: PA2826313975

Gene: PARN HGNC NCBI

ClinVar RCV:

RCV000484657

RCV001308486

RCV002509408

ClinVar Variation:

423824

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229921.1:p.Arg398Cys	CA7912056 NM_001242992.2:c.1192C>T