Canonical Allele Identifier: PA2826394109
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001838
ClinVar RCV Id: RCV001298184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Gln36His
CA7994474
NM_001256442.2:c.108G>C
CA395477313
NM_001256442.2:c.108G>T