Canonical Allele Identifier: PA1139759464
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 956024
ClinVar RCV Id: RCV001228756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Lys19Gln
CA7994470
NM_145239.3:c.55A>C