Canonical Allele Identifier: PA2826394220
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1312389
ClinVar RCV Id: RCV001755143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Asp143Glu
CA395478653
NM_001256442.2:c.429C>A
CA395478655
NM_001256442.2:c.429C>G