Allele Registry

Canonical Allele Identifier: PA658816980

Gene: PARN HGNC NCBI

ClinVar Variation Id: 542670

HGVS (amino-acid)	Matching Registered Transcripts
NP_002573.1:p.Lys615Glu	CA7911921 NM_002582.4:c.1843A>G