Canonical Allele Identifier: PA2826394221
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2043464
ClinVar RCV Id: RCV002895820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Asp143Tyr
CA395478645
NM_001256442.2:c.427G>T