Canonical Allele Identifier: PA2826394400
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452226
ClinVar RCV Id: RCV000519530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Phe288Leu
CA395480171
NM_001256442.2:c.862T>C
CA395480186
NM_001256442.2:c.864C>A
CA395480188
NM_001256442.2:c.864C>G