Allele Registry

Canonical Allele Identifier: PA645295019

Gene: PARN HGNC NCBI

ClinVar RCV:

RCV000484657

RCV001308486

RCV002509408

ClinVar Variation:

423824

HGVS (amino-acid)	Matching Registered Transcripts
NP_002573.1:p.Arg444Cys	CA7912056 NM_002582.4:c.1330C>T