Canonical Allele Identifier: PA317034
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65757
ClinVar RCV Id: RCV000055990 RCV000791448 RCV001332952 RCV001719806 RCV002354247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Pro216Arg
CA317033
NM_145239.3:c.647C>G