Canonical Allele Identifier: PA891859441
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 573345
ClinVar RCV Id: RCV000694996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ala183Pro
CA7994542
NM_145239.3:c.547G>C