Canonical Allele Identifier: PA2826394097
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1342734
ClinVar RCV Id: RCV001840845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Gly26Ala
CA395477179
NM_001256442.2:c.77G>C