Canonical Allele Identifier: PA2826394707
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1018328
ClinVar RCV Id: RCV001317612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Ile170Ser
CA395478850
NM_001256443.2:c.509T>G