Canonical Allele Identifier: PA2573302461
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1378743
ClinVar RCV Id: RCV001890232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Glu16Gln
CA395477058
NM_145239.3:c.46G>C