Canonical Allele Identifier: PA2499298016
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_660282.2:p.Gln36His
CA7994474
NM_145239.3:c.108G>C
CA395477313
NM_145239.3:c.108G>T