Canonical Allele Identifier: PA2826394668
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2043464
ClinVar RCV Id: RCV002895820
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Asp143Tyr
CA395478645
NM_001256443.2:c.427G>T