Canonical Allele Identifier: PA2573302500
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449898
ClinVar RCV Id: RCV002004712 RCV003418245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Glu169Gly
CA395478841
NM_145239.3:c.506A>G