Allele Registry

Canonical Allele Identifier: PA658816965

Gene: PARN HGNC NCBI

ClinVar RCV:

RCV000653141

RCV000850488

RCV001816642

RCV002223900

RCV003447549

RCV003994067

ClinVar Variation:

542669

HGVS (amino-acid)	Matching Registered Transcripts
NP_002573.1:p.Tyr91Cys	CA7912470 NM_002582.4:c.272A>G