Canonical Allele Identifier: PA2826394131
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 560656
ClinVar RCV Id: RCV000678832 RCV002232812
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Pro58Arg
CA395477551
NM_001256442.2:c.173C>G