Canonical Allele Identifier: PA2826394222
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 451350
ClinVar RCV Id: RCV000523548 RCV002231213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Pro144Leu
CA395478667
NM_001256442.2:c.431C>T