Canonical Allele Identifier: PA645448641
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418426
ClinVar RCV Id: RCV000482740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ser275Pro
CA16620190
NM_145239.3:c.823T>C