Canonical Allele Identifier: PA916076656
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 639782
ClinVar RCV Id: RCV000792681 RCV003317369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ala291Thr
CA395480227
NM_145239.3:c.871G>A