Allele Registry

Canonical Allele Identifier: PA2826394772

Gene: PRRT2 HGNC NCBI

ClinVar RCV:

RCV002573934

ClinVar Variation:

1898437

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243372.1:p.Gln221His	CA395479209 NM_001256443.2:c.663G>C CA395479210 NM_001256443.2:c.663G>T