Canonical Allele Identifier: PA2573099154
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1342734
ClinVar RCV Id: RCV001840845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Gly26Ala
CA395477179
NM_145239.3:c.77G>C