Canonical Allele Identifier: PA2826394739
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 206685
ClinVar RCV Id: RCV000800897 RCV001711482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.His201Gln
CA317023
NM_001256443.2:c.603C>G
CA395479046
NM_001256443.2:c.603C>A