Canonical Allele Identifier: PA2499298029
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1044105
ClinVar RCV Id: RCV001348313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ser28Cys
CA395477207
NM_145239.3:c.83C>G