Allele Registry

Canonical Allele Identifier: PA3057500769

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV005114464

ClinVar Variation:

3637379

HGVS (amino-acid)	Matching Registered Transcripts
NP_660282.2:p.Asp226Val	CA395479254 NM_145239.3:c.677A>T