Canonical Allele Identifier: PA1139759446
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 862416
ClinVar RCV Id: RCV001069135
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Glu16Lys
CA7994467
NM_145239.3:c.46G>A