Canonical Allele Identifier: PA2826394507
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2831859
ClinVar RCV Id: RCV003758285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Ala2Glu
CA7994459
NM_001256443.2:c.5C>A